N7S (p.Asn7Ser) variant of ABCC2 (Q92887)
N7S (p.Asn7Ser) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
N7S (p.Asn7Ser) variant details
- p.Asn7Ser
- TOPMed rs2037639136
- Missense
- Variant Prioritization Score for Impact Estimate 0.367
- CADD 18.50
- PolyPhen-2 0.05
- SIFT 0.13
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available